Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 088059
Company: AKORN
Company: AKORN
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| PREDAMIDE | PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM | 0.5%;10% | SUSPENSION/DROPS;OPHTHALMIC | Discontinued | None | No | No |
Original Approvals or Tentative Approvals
| Action Date | Submission | Action Type | Submission Classification | Review Priority; Orphan Status | Letters, Reviews, Labels, Patient Package Insert | Notes | Url |
|---|---|---|---|---|---|---|---|
| 07/29/1983 | ORIG-1 | Approval |
Label is not available on this site. |
Supplements
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
|---|---|---|---|---|---|
| 12/20/1990 | SUPPL-8 | Labeling |
Label is not available on this site. |
||
| 09/30/1988 | SUPPL-7 | Labeling |
Label is not available on this site. |
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| 03/01/1988 | SUPPL-5 | Labeling |
Label is not available on this site. |